WO2005113542A3 - Inhibiteurs sulfonamido n-cycliques de gamma-secretase - Google Patents
Inhibiteurs sulfonamido n-cycliques de gamma-secretase Download PDFInfo
- Publication number
- WO2005113542A3 WO2005113542A3 PCT/US2005/017985 US2005017985W WO2005113542A3 WO 2005113542 A3 WO2005113542 A3 WO 2005113542A3 US 2005017985 W US2005017985 W US 2005017985W WO 2005113542 A3 WO2005113542 A3 WO 2005113542A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inhibitors
- compounds
- gamma secretase
- formula
- cyclic sulfonamido
- Prior art date
Links
- 102000002659 Amyloid Precursor Protein Secretases Human genes 0.000 title 1
- 108010043324 Amyloid Precursor Protein Secretases Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 208000024827 Alzheimer disease Diseases 0.000 abstract 2
- 208000010877 cognitive disease Diseases 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/58—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems with hetero atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/50—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D263/57—Aryl or substituted aryl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/04—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D277/06—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pyrrole Compounds (AREA)
- Indole Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Quinoline Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05754201A EP1758884A2 (fr) | 2004-05-20 | 2005-05-20 | Inhibiteurs sulfonamido n-cycliques de gamma-secretase |
CA002567343A CA2567343A1 (fr) | 2004-05-20 | 2005-05-20 | Inhibiteurs sulfonamido n-cycliques de gamma-secretase |
JP2007527530A JP2007538106A (ja) | 2004-05-20 | 2005-05-20 | γセクレターゼのN−環式スルホンアミド阻害剤 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US57286204P | 2004-05-20 | 2004-05-20 | |
US60/572,862 | 2004-05-20 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2005113542A2 WO2005113542A2 (fr) | 2005-12-01 |
WO2005113542A3 true WO2005113542A3 (fr) | 2006-03-02 |
WO2005113542B1 WO2005113542B1 (fr) | 2006-04-20 |
Family
ID=34968952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2005/017985 WO2005113542A2 (fr) | 2004-05-20 | 2005-05-20 | Inhibiteurs sulfonamido n-cycliques de gamma-secretase |
Country Status (5)
Country | Link |
---|---|
US (1) | US20060035884A1 (fr) |
EP (1) | EP1758884A2 (fr) |
JP (1) | JP2007538106A (fr) |
CA (1) | CA2567343A1 (fr) |
WO (1) | WO2005113542A2 (fr) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE0302573D0 (sv) | 2003-09-26 | 2003-09-26 | Astrazeneca Ab | Benzimidazole derivatives, compositions containing them, preparation thereof and uses thereof |
FR2869904B1 (fr) * | 2004-05-07 | 2006-07-28 | Fournier S A Sa Lab | Modulateurs des recepteurs lxr |
EP1789404B1 (fr) * | 2004-06-30 | 2010-03-24 | Schering Corporation | Amines heterocycliques a substitution n-arylsulfonyle inhibant la gamma secretase |
ES2380709T3 (es) | 2004-09-24 | 2012-05-17 | Astrazeneca Ab | Derivados de bencimidazol, composiciones que los contienen, su preparación y usos |
WO2006094633A1 (fr) * | 2005-03-03 | 2006-09-14 | F. Hoffman-La Roche Ag | Derives d’amide d’acide 1-sulfonyl-piperdine-3-carboxylique en tant qu’inhibiteurs de la 11-beta-hydroxysteroide dehydrogenase pour le traitement du diabete sucre de type ii |
JP2009507800A (ja) * | 2005-09-09 | 2009-02-26 | ユーロ−セルティーク エス.エイ. | 縮合およびスピロ環化合物ならびにその使用 |
PE20071090A1 (es) * | 2005-12-01 | 2007-10-24 | Elan Pharm Inc | 5-pirazolpiperidinas-(sustituidas) |
JP2009519933A (ja) * | 2005-12-14 | 2009-05-21 | アムゲン インコーポレイティッド | ジアザ複素環式スルホンアミド誘導体およびそれらの使用法 |
GB0526257D0 (en) * | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
WO2007092435A2 (fr) | 2006-02-07 | 2007-08-16 | Wyeth | Inhibiteurs 11-beta hsd1 |
JP2009526065A (ja) * | 2006-02-08 | 2009-07-16 | ワイス | C型肝炎ウイルスによる感染を治療するためのスルホンアミド誘導体 |
KR20080114711A (ko) * | 2006-03-02 | 2008-12-31 | 아스텔라스세이야쿠 가부시키가이샤 | 17β HSD 타입 5 저해제 |
TW200745049A (en) | 2006-03-23 | 2007-12-16 | Astrazeneca Ab | New crystalline forms |
TW200808769A (en) | 2006-04-18 | 2008-02-16 | Astrazeneca Ab | Therapeutic compounds |
TW200813054A (en) * | 2006-06-02 | 2008-03-16 | Elan Pharm Inc | Fused, tricyclic sulfonamide inhibitors of gamma secretase |
ATE509956T1 (de) * | 2006-06-08 | 2011-06-15 | Helmholtz Zentrum Muenchen | Spezifische proteaseinhibitoren und ihre verwendung in der krebstherapie |
PT2066659E (pt) * | 2006-09-29 | 2013-11-07 | Gruenenthal Gmbh | Derivados de sulfonamida substituídos |
WO2008100412A1 (fr) * | 2007-02-12 | 2008-08-21 | Merck & Co., Inc. | Dérivés de la pipéridine |
GB0813144D0 (en) | 2008-07-17 | 2008-08-27 | Glaxo Group Ltd | Novel compounds |
GB0813142D0 (en) | 2008-07-17 | 2008-08-27 | Glaxo Group Ltd | Novel compounds |
ES2439767T3 (es) | 2008-08-01 | 2014-01-24 | Purdue Pharma Lp | Compuestos de tetrahidropiridinilo y dihidropirrolilo y uso de los mismos |
CN102203089A (zh) * | 2008-09-05 | 2011-09-28 | 伊兰医药品公司 | N-磺酰氨基多环吡唑基化合物 |
WO2011073273A1 (fr) * | 2009-12-16 | 2011-06-23 | Evotec Ag | Dérivés d'arylsulfonamides de benzoxazine en tant que modulateurs de kv.1.3 |
WO2011073276A1 (fr) * | 2009-12-16 | 2011-06-23 | Evotec Ag | Dérivés d'arylsulfonamides de benzoxazine en tant que modulateurs de kv.1.3 |
GB201000685D0 (en) | 2010-01-15 | 2010-03-03 | Glaxo Group Ltd | Novel compounds |
US20150291517A1 (en) * | 2012-11-28 | 2015-10-15 | Martijn Fiers | Benzenesulfonamide compounds for somatic embryogenesis in plants |
WO2014134705A1 (fr) * | 2013-03-04 | 2014-09-12 | Advanced Medical Research Institute Of Canada | Dérivés de la sulfonyle quinoléine et applications associées |
JP6506291B2 (ja) * | 2013-09-10 | 2019-04-24 | ボード オブ リージェンツ オブ ザ ユニヴァーシティ オブ テキサス システム | 短縮型大腸腺腫性ポリポーシス(apc)タンパク質を標的にする治療剤 |
CN104557664B (zh) * | 2013-10-19 | 2020-01-21 | 广东东阳光药业有限公司 | 芳杂环类衍生物及其在药物上的应用 |
CN104557726B (zh) * | 2013-10-19 | 2019-05-24 | 广东东阳光药业有限公司 | 芳杂环类衍生物及其在药物上的应用 |
WO2015090233A1 (fr) | 2013-12-20 | 2015-06-25 | Sunshine Lake Pharma Co., Ltd. | Composés hétérocycliques aromatiques et leur utilisation dans les produits pharmaceutiques |
CN105085367B (zh) * | 2014-05-03 | 2019-05-21 | 广东东阳光药业有限公司 | 取代的杂芳基化合物及其组合物和用途 |
US10082496B2 (en) | 2014-09-10 | 2018-09-25 | Board Of Regents Of The University Of Texas System | Targeting emopamil binding protein (EBP) with small molecules that induce an abnormal feedback response by lowering endogenous cholesterol biosynthesis |
CN105732459B (zh) * | 2014-12-29 | 2019-05-31 | 成都先导药物开发有限公司 | 吡咯酰胺类化合物及其制备方法与用途 |
CN105801464B (zh) | 2014-12-29 | 2019-05-28 | 成都先导药物开发有限公司 | 吡咯酰胺类化合物及其制备方法与用途 |
WO2016107542A1 (fr) * | 2014-12-29 | 2016-07-07 | 成都先导药物开发有限公司 | Composé pyrrole amide, son procédé de préparation et son utilisation |
WO2016107544A1 (fr) * | 2014-12-29 | 2016-07-07 | 成都先导药物开发有限公司 | Composé intermédiaire pour la préparation d'un composé pyrrole amide et son procédé de préparation et d'utilisation |
SG11201811023UA (en) | 2016-06-23 | 2019-01-30 | St Jude Childrens Res Hospital | Small molecule modulators of pantothenate kinases |
JP2019532054A (ja) | 2016-09-20 | 2019-11-07 | グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー2)、リミテッドGlaxosmithkline Intellectual Property (No.2) Limited | Trpv4拮抗薬 |
TW201825458A (zh) | 2016-09-20 | 2018-07-16 | 英商葛蘭素史克智慧財產(第二)有限公司 | Trpv4拮抗劑 |
CA3036933A1 (fr) | 2016-09-20 | 2018-03-29 | Glaxosmithkline Intellectual Property (No.2) Limited | Antagonistes de trpv4 |
BR112020012875A2 (pt) | 2017-12-27 | 2021-01-05 | St. Jude Children¿S Research Hospital, Inc. | Moduladores de pequenas moléculas das pantotenato quinases |
EP3731859A4 (fr) | 2017-12-27 | 2021-09-22 | St. Jude Children's Research Hospital, Inc. | Méthodes de traitement de troubles associés à castor |
KR102068299B1 (ko) * | 2018-12-21 | 2020-01-20 | 한국기초과학지원연구원 | Cyp4a 저해 화합물을 유효성분으로 포함하는 대사질환의 예방 또는 치료용 조성물 |
CN109925510A (zh) * | 2019-04-11 | 2019-06-25 | 北京卓凯生物技术有限公司 | Rac1活性抑制剂在制备治疗阿尔茨海默病的药物中的应用 |
GB201918410D0 (en) * | 2019-12-13 | 2020-01-29 | Z Factor Ltd | Compounds and their use for the treatment of alpha1-antitrypsin deficiency |
EP3868376A1 (fr) * | 2020-02-21 | 2021-08-25 | Institut national de recherche pour l'agriculture, l'alimentation et l'environnement | Procédé de traitement d'infections bactériennes et composition pharmaceutique pour le traitement d'infections bactériennes |
GB202108543D0 (en) * | 2021-06-15 | 2021-07-28 | Z Factor Ltd | Compounds and their use for the treatment of alpha1-antitrypsin deficiency |
GB202108544D0 (en) * | 2021-06-15 | 2021-07-28 | Z Factor Ltd | Compounds and their use for the treatment of alpha1-antitrypsin deficiency |
GB202108542D0 (en) * | 2021-06-15 | 2021-07-28 | Z Factor Ltd | Compounds and their use for the treatment of alpha1-antitrypsin deficiency |
EP4450494A1 (fr) | 2023-04-20 | 2024-10-23 | Consejo Superior De Investigaciones Científicas | Dérivés d'indole en tant qu'inhibiteurs d'histone désacétylase (hdac) pour le traitement du cancer |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003014075A2 (fr) * | 2001-08-03 | 2003-02-20 | Schering Corporation | Nouveaux inhibiteurs de gamma-secretase |
WO2003066592A1 (fr) * | 2002-02-06 | 2003-08-14 | Schering Corporation | Inhibiteurs de la gamma-secretase |
WO2003093245A1 (fr) * | 2002-05-03 | 2003-11-13 | Elan Pharmaceuticals, Inc. | Derives d'acetamide sulfonylquinoxalone et composes associes en tant qu'antagonistes de la bradykinine |
WO2005068448A1 (fr) * | 2003-08-29 | 2005-07-28 | Ionix Pharmaceuticals Limited | Sulfonamides a action antagoniste sur des canaux calcium de type n |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW575561B (en) * | 1999-03-25 | 2004-02-11 | Hoffmann La Roche | 1-arenesulfonyl-2-aryl-pyrrolidine and piperidine derivatives |
US6589978B2 (en) * | 2000-06-30 | 2003-07-08 | Hoffman-La Roche Inc. | 1-sulfonyl pyrrolidine derivatives |
-
2005
- 2005-05-20 US US11/133,738 patent/US20060035884A1/en not_active Abandoned
- 2005-05-20 EP EP05754201A patent/EP1758884A2/fr not_active Withdrawn
- 2005-05-20 WO PCT/US2005/017985 patent/WO2005113542A2/fr not_active Application Discontinuation
- 2005-05-20 JP JP2007527530A patent/JP2007538106A/ja active Pending
- 2005-05-20 CA CA002567343A patent/CA2567343A1/fr not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003014075A2 (fr) * | 2001-08-03 | 2003-02-20 | Schering Corporation | Nouveaux inhibiteurs de gamma-secretase |
WO2003066592A1 (fr) * | 2002-02-06 | 2003-08-14 | Schering Corporation | Inhibiteurs de la gamma-secretase |
WO2003093245A1 (fr) * | 2002-05-03 | 2003-11-13 | Elan Pharmaceuticals, Inc. | Derives d'acetamide sulfonylquinoxalone et composes associes en tant qu'antagonistes de la bradykinine |
WO2005068448A1 (fr) * | 2003-08-29 | 2005-07-28 | Ionix Pharmaceuticals Limited | Sulfonamides a action antagoniste sur des canaux calcium de type n |
Also Published As
Publication number | Publication date |
---|---|
US20060035884A1 (en) | 2006-02-16 |
WO2005113542A2 (fr) | 2005-12-01 |
CA2567343A1 (fr) | 2005-12-01 |
EP1758884A2 (fr) | 2007-03-07 |
JP2007538106A (ja) | 2007-12-27 |
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